Individual ID: 28867142.38

Individual ID	28867142.38
Pubmed ID	28867142
Whose mosaic mutation	Male Patient
Origin of mosaic mutation in patients	de novo
Phenotypic Category	3
Disease	Autism Spectrum Disorders(view all the variants in this disease)
OMIM ID	209850

Variants

Found 11 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
1217	933	CD22	19	35832660	35832660	Autism Spectrum Disorders	NextSeq500 v2
1246	23002	DAAM1	14	59791152	59791152	Autism Spectrum Disorders	NextSeq500 v2
1253	1756	DMD	X	32383221	32383221	Autism Spectrum Disorders	NextSeq500 v2
1397	3720	JARID2	6	15374368	15374368	Autism Spectrum Disorders	NextSeq500 v2
1406	57576	KIF17	1	21031010	21031010	Autism Spectrum Disorders	NextSeq500 v2
29786	29964	PRICKLE4	6	41751917	41751917	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29787	647024	C6orf132	6	42073489	42073489	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29788	54511	HMGCLL1	6	55364076	55364076	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29789	3617	IMPG1	6	76660802	76660802	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29790	6885	MAP3K7	6	91226345	91226345	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500
29807	4885	NPTX2	7	98256629	98256629	Autism Spectrum Disorders	NextSeq500 v2 NextSeq500